A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660728



Internal ID21609033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20980260..20980260hg38UCSC Ensembl
chr16:20991582..20991582hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097422
SamplesHG00171
Known GenesDNAH3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660728
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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